Substituted Methyl 5β-Cholan-24-oates; Part III: Synthesis of a Novel Cholaphane from Ethylene Glycol Diester of Lithocholic Acid by Cyclization with Terephthalic Acid

Erkki Kolehmainen, Jari Tamminen, Kari Lappalainen, Tuire Torkkel, Raimo Seppälä

Synthesis · 1996 · 24 citations · 0 references

Concepts

Abstract

A novel cholaphane, containing both an aliphatic and an aromatic spacer, has been prepared from ethylene glycol diester of 3α-hydroxy-5β-cholan-24-oic acid (lithocholic acid) by cyclization (Yamaguchi method) with terephthalic acid.